Heartline Gemini Dissection Forceps 2800-7828L

GUDID 00192896121980

Rigid endoscopic tissue manipulation forceps, reusable

Primary Device ID	00192896121980
NIH Device Record Key	b32629c2-94bf-40bc-9f3e-cac522451cc5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Heartline Gemini Dissection Forceps
Version Model Number	2800-7828L
Catalog Number	2800-7828L
Company DUNS	040729840
Company Name	SONTEC INSTRUMENTS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00192896121980 [Primary]

GCJ	Laparoscope, general & plastic surgery

Steralize Prior To Use	true
Device Is Sterile	false

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

[00192896121980]

Dry Heat Sterilization

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